Department of Immunology, Center for Cancer Immunology Research, The University of Texas MD Anderson Cancer Center, TX 77004, USA.
Allergol Int. 2012 Mar;61(1):19-25. doi: 10.2332/allergolint.11-RAI-0394. Epub 2012 Jan 25.
In an immune system, dendritic cells (DCs) are professional antigen-presenting cells (APCs) as well as powerful sensors of danger signals. When DCs receive signals from infection and tissue stress, they immediately activate and instruct the initiation of appropriate immune responses to T cells. However, it has remained unclear how the tissue microenvironment in a steady state shapes the function of DCs. Recent many works on thymic stromal lymphopoietin (TSLP), an epithelial cell-derived cytokine that has the strong ability to activate DCs, provide evidence that TSLP mediates crosstalk between epithelial cells and DCs, involving in DC-mediated immune homeostasis. Here, we review recent progress made on how TSLP expressed within the thymus and peripheral lymphoid and non-lymphoid tissues regulates DC-mediated T-cell development in the thymus and T-cell homeostasis in the periphery.
在免疫系统中,树突状细胞 (DC) 既是专业的抗原呈递细胞 (APC),也是危险信号的强大传感器。当 DC 接收到来自感染和组织应激的信号时,它们会立即被激活,并指导 T 细胞启动适当的免疫反应。然而,组织微环境在稳定状态下如何塑造 DC 的功能仍不清楚。最近关于胸腺基质淋巴生成素 (TSLP) 的许多研究工作表明,TSLP 是一种上皮细胞衍生的细胞因子,具有强烈激活 DC 的能力,为 TSLP 介导上皮细胞和 DC 之间的串扰提供了证据,涉及 DC 介导的免疫稳态。在这里,我们综述了 TSLP 在胸腺和外周淋巴和非淋巴组织中的表达如何调节胸腺中 DC 介导的 T 细胞发育以及外周 T 细胞稳态的最新进展。